| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4165404 | The Journal of Pediatrics | 2013 | 9 Pages |
Abstract
Much of the observed UCH could be attributed to variation at the UGT1A1 locus, and UGT1A1 testing helped to substantiate a genetic diagnosis, thereby aiding in individual and family disease management. Although UGT1A1 variation plays a large role in UCH, genetic assessment of UGT1A1 alone may not be comprehensive. Assessment of additional genes may also be useful to evaluate genetic causes for UCH.
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Authors
Jennifer M. BS, Katrina E. MS, Susan A. BS, Dennis J. PhD, Linnea M. PhD,